AU2004247684B2 - Polyvinyl butyral sheet with bifunctional surface modifying agent - Google Patents

Polyvinyl butyral sheet with bifunctional surface modifying agent Download PDF

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AU2004247684B2
AU2004247684B2 AU2004247684A AU2004247684A AU2004247684B2 AU 2004247684 B2 AU2004247684 B2 AU 2004247684B2 AU 2004247684 A AU2004247684 A AU 2004247684A AU 2004247684 A AU2004247684 A AU 2004247684A AU 2004247684 B2 AU2004247684 B2 AU 2004247684B2
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polymer sheet
segment
modifying agent
surface modifying
compatibility
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AU2004247684A1 (en
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Wenjie Chen
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Solutia Inc
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Solutia Inc
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J7/00Chemical treatment or coating of shaped articles made of macromolecular substances
    • C08J7/04Coating
    • C08J7/06Coating with compositions not containing macromolecular substances
    • C08J7/065Low-molecular-weight organic substances, e.g. absorption of additives in the surface of the article
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D1/00Processes for applying liquids or other fluent materials
    • B05D1/02Processes for applying liquids or other fluent materials performed by spraying
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B05SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05DPROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
    • B05D1/00Processes for applying liquids or other fluent materials
    • B05D1/18Processes for applying liquids or other fluent materials performed by dipping
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/10009Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets
    • B32B17/10036Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets comprising two outer glass sheets
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/1055Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
    • B32B17/10761Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing vinyl acetal
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/10807Making laminated safety glass or glazing; Apparatus therefor
    • B32B17/10899Making laminated safety glass or glazing; Apparatus therefor by introducing interlayers of synthetic resin
    • B32B17/10935Making laminated safety glass or glazing; Apparatus therefor by introducing interlayers of synthetic resin as a preformed layer, e.g. formed by extrusion
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B32LAYERED PRODUCTS
    • B32BLAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
    • B32B17/00Layered products essentially comprising sheet glass, or glass, slag, or like fibres
    • B32B17/06Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
    • B32B17/10Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
    • B32B17/10005Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
    • B32B17/10807Making laminated safety glass or glazing; Apparatus therefor
    • B32B17/10981Pre-treatment of the layers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J5/00Manufacture of articles or shaped materials containing macromolecular substances
    • C08J5/18Manufacture of films or sheets
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L29/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal or ketal radical; Compositions of hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Compositions of derivatives of such polymers
    • C08L29/14Homopolymers or copolymers of acetals or ketals obtained by polymerisation of unsaturated acetals or ketals or by after-treatment of polymers of unsaturated alcohols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2329/00Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an alcohol, ether, aldehydo, ketonic, acetal, or ketal radical; Hydrolysed polymers of esters of unsaturated alcohols with saturated carboxylic acids; Derivatives of such polymer
    • C08J2329/14Homopolymers or copolymers of acetals or ketals obtained by polymerisation of unsaturated acetals or ketals or by after-treatment of polymers of unsaturated alcohols
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00Use of organic ingredients
    • C08K5/36Sulfur-, selenium-, or tellurium-containing compounds
    • C08K5/41Compounds containing sulfur bound to oxygen
    • C08K5/42Sulfonic acids; Derivatives thereof
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31598Next to silicon-containing [silicone, cement, etc.] layer
    • Y10T428/31601Quartz or glass
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31627Next to aldehyde or ketone condensation product
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31627Next to aldehyde or ketone condensation product
    • Y10T428/3163Next to acetal of polymerized unsaturated alcohol [e.g., formal butyral, etc.]
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31551Of polyamidoester [polyurethane, polyisocyanate, polycarbamate, etc.]
    • Y10T428/31645Next to addition polymer from unsaturated monomers
    • Y10T428/31649Ester, halide or nitrile of addition polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31935Ester, halide or nitrile of addition polymer
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T428/00Stock material or miscellaneous articles
    • Y10T428/31504Composite [nonstructural laminate]
    • Y10T428/31855Of addition polymer from unsaturated monomers
    • Y10T428/31938Polymer of monoethylenically unsaturated hydrocarbon

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Manufacturing & Machinery (AREA)
  • Materials Engineering (AREA)
  • Laminated Bodies (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
  • Joining Of Glass To Other Materials (AREA)

Description

23, Dec. 2008 15:20 Baldwins 64 4 4736712 No, 4079 P. 6 00 0 POLYVINYL BUTYRAL SHEET WITH BIFUNCTIONAL o SURFACE MODIFYING AGENT [0001] This disclosure relates to polymer sheets and, more particularly, to polymer 0 sheets comprising polyvinyl butyral having enhanced blocking resistance provided via a Ci bifunctional surface modifying agent disposed at a surface of the polyvinyl butyral sheets.
BACKGROUND
00 00 10002] Any discussion of the prior art throughout the specification should in no way be Sonsidered as m admission that such prior art is widely known or forms part of common general knowledge in the field.
S IOOta] Plasticized polyvinyl butyral (hereinafter "PVB") is commonly used in the ^1 manufacture of polymer sheets for use as interlayers in light transmitting laminates such as safety glass or polymeric laminates. Safety glass typically refers to a transparent laminate comprised of a polyvinyl bu*tyr sheet sandwiched between two panes of glass. Safety glass often is used to provide a transparent barrier in architectural and automotive openings. Its main function is to absorb energy, such as caused by a blow from an object, without allowing penetration through the opening, thus minimizing damage or injury to the objects or persons within an enclosed area. Additives to the sheet formulation generally include adhesion control agents to modify adhesion of the sheet to the glass so that a suitable level of adhesion can be maintained so as t prevent spalling of the glass and yet provide adequate energy absorption on impact. The interlayer sheet also may be modified to impart additional beneficial effects to safety glass such as to attenuate acoustic noise, reduce UV and/or IR light transmission, and/or enhance the aesthetic appeal of window openings.
[0003] Safety glass typically is formed by a process in which two layers of glass and a plastic interlayer, such as PVB, are assembled into a prm-press, tacked into a pre-laminate, and finished into an optically clear laminate, The assembly phase involves laying down a piece of glass, overlaying a PVB sheet, laying down a second piece of glass, and then trimming the excess PVB to the edges of the glass layers, [0004] The plastic iterlayer generally is produced by mixing PVB polymer with one or more plasticizers, and optionally with one or more other ingredients, and melt processing the mix into sheeting, which typically is collected and rolled for storage and transportation.
In the lamination process for automotive windscreens, sections of PVB sheet typically are cut from the roll and these cut sections are shaped and/or stacked for assembly. A cut section then is taken from the stack and assembled in layered arrangement with a rigid substrate I COMS ID No: ARCS-218225 Received by IP Australia: Time 14:30 Date 2008-12-23 WO 2004/111116 PCT/US2004/017953 glass sheet having a particular optical quality) such that a face of the rigid substrate and a face of the cut section are disposed in intimate contact and form a pre-press laminate assembly. Alternatively, this laminate assembly may be formed by interleaving multiple cut section(s) with multiple rigid sheets.
[0005] Plasticized PVB sheet, whether in roll form or in stacked form, inherently tends to stick to itself ("block") at ambient temperatures typically encountered before and during the laminating process. Many attempts to enhance the blocking resistance of PVB have been made, including mechanical roughing of the sheet surfaces embossing), applying a powder such as sodium bicarbonate to the sheet surfaces, and chemically or physically treating the surfaces of the PVB sheeting. Such surface treatments unfortunately often introduce undesirable handling or glass adhesion issues. In another common practice to avoid such blocking, the PVB sheeting may be interleaved with another sheet material, such as polyethylene, or may be stored and transported under refrigeration, at temperatures from about 5 to about 15 However, for variations of standard PVB sheeting, such as PVB sheeting incorporating high plasticizer content to accomplish an enhanced noise reduction (acoustic) function, blocking may occur even under refrigeration conditions.
[0006] Additionally, it has been proposed to incorporate various blocking-resistant materials into the PVB. Incorporation of such materials into the PVB, however, may adversely affect the optical properties of the resulting laminate or the adhesive properties of the PVB sheet to glass.
[0007] Accordingly, further improved methods are needed to enhance the blocking resistance of PVB" sheet, without adversely affecting optical clarity of laminates and glass adhesion properties of the resulting PVB sheet.
SUMMARY
[0008] It now surprisingly has been discovered, according to the present invention, that a polymer sheet comprising a bifunctional surface modifying agent disposed onto said polymer sheet surface results in enhanced antiblock characteristics without adverse optical and adhesion effects. Also, it has been discovered that antiblocking characteristics may be imparted to a surface of a polymer sheet by a method of manufacture comprising disposing a bifunctional surface modifying agent onto a surface of said polymer sheet. Further, the present invention includes a laminated safety glass comprising two sheets of glass with an interlayer polymer sheet disposed therebetween wherein the polymer sheet has a bifunctional surface modifying agent disposed onto a surface of said polymer sheet.
0 b i In one aspect of the invention there is provided a polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising, an anti-blocking segment; and a compatibility segment, wherein said bifunctional surface modifying agent comprises the sodium salt of 00 dodecylbenzenesulfonic acid.
In another aspect of the invention there is provided a laminated safety glass comprising two sheets of glass with an interlayer polymer sheet disposed therebetween, wherein the polymer sheet has a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising an anti-blocking segment and a compatibility segment, wherein said bifunctional surface modifying agent comprises the sodium salt of dodecylbenzenesulfonic acid.
In another aspect of the invention there is provided a polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a sulfonate radical and wherein said compatibility segment further comprises a positively charged alkali metal counter ion.
In another aspect of the invention there is provided a laminated safety glass comprising two sheets of glass with an interlayer polymer sheet disposed therebetween, wherein the polymer sheet has a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a sulfonate radical and wherein said compatibility segment further comprises an alkali metal positively charged counter ion.
In another aspect of the invention there is provided a polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a carboxylate radical and wherein said compatibility segment further comprises a positively charged alkali metal counter ion.
In another aspect of the invention there is provided a laminated safety glass N comprising two sheets of glass with an interlayer polymer sheet disposed therebetween, z wherein the polymer sheet has a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a carboxylate radical and wherein said compatibility segment further comprises an alkali metal O0 positively charged counter ion.
N In another aspect of the invention there is provided a polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional N surface modifying agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a phosphate radical and wherein said compatibility segment further comprises a positively charged alkali metal counter ion.
In another aspect of the invention there is provided a laminated safety glass comprising two sheets of glass with an interlayer polymer sheet disposed therebetween, wherein the polymer sheet has a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a phosphate radical and wherein said compatibility segment further comprises an alkali metal positively charged counter ion.
In another aspect of the invention there is provided a polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a sulfonate, sulfate, carboxylate, or phosphate radical and wherein said compatibility segment further comprises a positively charged alkali metal counter ion; wherein said anti-blocking segment comprises a benzyl group.
followed by page 3 23. Dec. 2008 15:29 Baldwins 64 4 4736712 No. 4079 P. 7 o 10009] Disclosed herein are exemplary embodiments of polymer sheets having o bifunctional surface modifying agents disposed at surfaces, methods of manufacturing polymer 0 sheets having a bifunctional surface modifying agent disposed at surfaces, and methods of 0 enhancing the blocking resistance of polymer sheets. In one embodiment, the polymer sheet comprises polyvinyl butyral, a plasticizer incorporated into the polyvinyl butyral, and a Ci bifiunctional surface modifying agent disposed onto the plasticized polyvinyl butyral surfaces.
The biftmnctional surface modifying agent comprises an anti-blocking segment and a compatibility segment. The anti-blocking segment comprises a hydrocarbon group such as a IN linear hydrocarbon chain. The compatibility segment comprises a polar group such as a sulfonate, sulfate, carboxylate, or phosphate radical. The anti-blocking and compatibility segments provide therefore the bi-functions of anti-blocking and compatibility to the polymer o sheet respectively to the agent C, [10010] A method of manufacturing a polymer sheet comprises melt-processing a polymer into a sheet and disposing a bifunctional surface modifying agent onto the polymer sheet surfaces, the bifunctional surface modifying agent comprising an anti-blocking segment and a compatibility segment The anti-blocking segment comprises a hydrocarbon group such as a linear hydrocarbon chain. The compatibility segment comprises a polar group such as a sulfonate, sulfate, carboxylate, or phosphate radical.
[00111 A laminated safety glass comprises two sheets of glass with an interlayer polymer sheet disposed thercbetween wherein the polymer sheet has a bifunctional surface modifying agent disposed onto said polymer sheet surface, said bifunctional surface modifying agent comprising, an anti-blooking segment, and a compatibility segment.
DETAILED DESCRIPTION [0012] Unless the context clearly requires otherwise, throughout the description and the claims, the words 'comprise', 'comprising', and the like are to be construed in an inclusive sense as opposed to an exclusive or exhaustive sense; that is to say, in the sense of 'including, but not limited to".
[0012a] A plasticized polymer in sheet form, according to the present invention, has a bifmenctional surface modifying agent disposed at the surface of the polymer sheet Although the embodiments described below refer to the polymer as being PVB, it should be understood that the polymer may be any polymer having a suitable glass transition temperature. Typical such polymers include polyvinyl butyral, polyurethane, polyvinyl chloride, poly(ethylen.e-covinyl acetate), combinations of the foregoing, and the like. The bifunctional surface modifying agent enhances the blocking resistance of the polymer sheet and comprises an COMS ID No: ARCS-218225 Received by IP Australia: Time 14:30 Date 2008-12-23 WO 2004/111116 PCT/US2004/017953 anti-blocking segment and a compatibility segment. The anti-blocking segment comprises a hydrocarbon group such as a linear hydrocarbon chain. The compatibility segment comprises a polar group such as a sulfonate, sulfate, carboxylate, or phosphate radical that imparts suitable affinity to the polymer sheet.
[0013] PVB generally is produced by known acetalization processes which involve reacting PVOH with butyraldehyde in the presence of acid catalyst, followed by neutralization of the catalyst, separation, stabilization and drying of the resin. The polymer typically comprises about 13 to about 30 weight percent (wt. hydroxyl groups calculated as PVOH, and preferably about 15 to about 22 wt. hydroxyl groups calculated as PVOH.
The polymer further comprises up to about 10 wt. residual ester groups and preferably up to about 3 wt. residual ester groups calculated as polyvinyl acetate with the balance being an acetal, preferably butyraldehyde acetal, but optionally including other acetal groups, a 2-ethyl hexanal- group. Typically, the product PVB has a molecular weight greater than about 70,000 grams per mole (g/mole). As used herein, the term "molecular weight" should be construed as the average molecular weight. Details of suitable processes for making PVB are known to those skilled in the art. PVB is commercially available from Solutia Inc., St.
Louis, Missouri as ButvarTM resin.
[0014] Additives may be added to the PVB polymer to enhance its performance in a final product. Such additives include, but are not limited to, dyes, pigments, stabilizers ultraviolet stabilizers), antioxidants, combinations of the foregoing additives, and the like.
[0015] The PVB sheet typically comprises about 20 to 80, and more commonly 25 to parts plasticizer per one hundred parts of resin The amount of plasticizer affects the Tg of the PVB sheet. Normally, increasing the amount of plasticizer decreases the T,.
Generally, the PVB sheets have a Tg of about 30 °C or less. PVB sheets having a Tg lower than about 20°C are often used as acoustic PVB sheets. Plasticizers commonly employed are esters of a polybasic acid or a polyhydric alcohol. Suitable plasticizers include, for example, triethylene glycol di-(2-ethylbutyrate), triethylene glycol di-(2-ethylhexanoate), triethylene glycol diheptanoate, tetraethylene glycol diheptanoate, dihexyl adipate, dioctyl adipate, hexyl cyclohexyladipate, mixtures of heptyl and nonyl adipates, diisononyl adipate, heptylnonyl adipate, dibutyl sebacate, polymeric plasticizers such as the oil-modified sebacic alkyds, and mixtures of phosphates and adipates such as disclosed in U.S. Pat. No. 3,841,890 and adipates such as disclosed in U.S. Pat. No. 4,144,217. Also commonly employed plasticizers are mixed adipates made from C 4 to C, alkyl alcohols and cyclo C 4 to CIo alcohols, as WO 2004/111116 PCT/US2004/017953 disclosed in U.S. Pat. No. 5,013,779. C 6 to C, adipate esters, such as dihexyl adipate, are preferred plasticizers.
[0016] The PVB polymer and plasticizer additives are thermally processed and configured into sheet form. One exemplary method of forming a PVB sheet comprises extruding molten PVB resin plasticizer additives (hereinafter "melt") by forcing the melt through a sheet die a die having an opening that is substantially greater in one dimension than in a perpendicular dimension). Another exemplary method of forming a PVB sheet comprises casting molten resin or semi-molten resin from a die onto a roller, solidifying the resin, and subsequently removing the solidified resin as a sheet. In either embodiment, the surface texture at either or both sides of the sheet may be controlled by adjusting the surfaces of the die opening or by providing texture at the roller surface. Other techniques for controlling the sheet texture include varying parameters of the reactant materials the water content of the resin and/or the plasticizer, the melt temperature, or combinations of the foregoing parameters). Furthermore, the sheet can be configured to include spaced projections that define a temporary surface irregularity to facilitate the de-airing of the sheet during lamination processes after which the elevated temperatures and pressures of the laminating process cause the projections to melt into the sheet, thereby resulting in a smooth finish. In any embodiment, the extruded sheets typically have thicknesses of about 0.3 to about 2.5 millimeters (mm).
[0017] The bifunctional surface modifying agent preferably is disposed as a coating at the surfaces of the PVB sheet and comprises an anti-blocking segment and a compatibility segment. Exemplary embodiments of modifying agents include alkylbenzenesulfonates
(RCH
4
SO
3 alkylsulfonates (RSO 3 alky sulfates (ROSO 3 alkylcarboxylates (RCOOM), polyalkoxycarboxylates (R(OCHCH 2
),OCH
2 COOM), and alkylphosphate esters
(ROPO
3 where M is hydrogen or a metal cation sodium, potassium, magnesium, calcium, and the like) or an ammonium ion, R is an alkyl group, and n, the number of repeat unit, is Preferably, the agent includes at least one sulfonate radical. In a preferred exemplary embodiment, as is shown below, the anti-blocking segment is X and the compatibility segment is a sulfonate group having a positively-charged counter ion Y disposed at the sulfonate group (-SO 3 The resultant structure is of the form X SO 3
Y
WO 2004/111116 PCT/US2004/017953 wherein X is a hydrocarbon group and Y is hydrogen, an ammonium ion, or an alkali metal ion. In particular, the hydrocarbon group is an aliphatic group, an aromatic group, or a combination of aliphatic and aromatic groups a linear hydrocarbon chain, a cyclic group a benzyl group), or a combination thereof) having at least about 8 carbon atoms and more preferably about 8 to about 50 carbon atoms. Preferably, the anti-blocking segment X is an aliphatic-aromatic compound having a molecular structure that imparts suitable antiblocking properties to the polymer sheet and is of the form R wherein R is a linear hydrocarbon chain having about 2 to about 44 carbon atoms.
[0018] The compatibility segment of the modifying agent the -SO 3 on the other hand, has a sufficient degree of affinity with the PVB sheet to provide the modifying agent a degree of compatibility with the PVB sheet to avoid or at least minimize adverse effects on the optical characteristics of the PVB sheet while effectively enhancing the blocking resistance of the PVB sheet. In particular, suitable polar groups exhibit sufficient affinity to the PVB sheet to enable the modifying agent to form a homogeneous thin coating on the PVB surface so that the light scattering tendencies through the PVB are minimized.
[0019] Preferred compounds for use as bifunctional surface modifying agents are aliphatic-aromatic sulfonates. Especially preferred is dodecylbenzenesulfonic acid (hereinafter referred to as which is of the formula
CH
3 (C H 2 )11SO 3
H
and sodium or magnesium salts of dodecylbenzenesulfonic acid (hereinafter referred to as "DSNa" or "DSMg"), one exemplary embodiment of which is of the formula
CH
3
(CH
2 11
SO
3 Na (or Mg) and which may be used in combination with DSH.
WO 2004/111116 PCTiUS2004/017953 [0020] Exemplary techniques of disposing the bifunctional surface modifying agent onto the PVB sheet surface include, but are not limited to, the physical application of the agent to the sheet surface. Physical applications of the agent include, but are not limited to, spray coating techniques, immersion (dipping) techniques, gravure coating techniques, and the like. In one exemplary spray coating technique, the agent is disposed dispersed or dissolved) in a liquid carrier, atomized, and projected to at least a portion of at least one side of the surfaces of the PVB sheet. The carrier may be aqueous or solvent-based ethanol, methanol, acetone, methyl ethyl ketone, combinations of the foregoing, and the like). Once deposited at the PVB sheet, the carrier is volatilized off, thereby leaving the modifying agent deposited on the surface of the PVB sheet. The concentration of modifying agent in the carrier should be sufficient to achieve the desired concentration of agent at the surface of the sheet In a typical spray technique, the concentration of bifunctional surface modifying agent in the carrier is about 0.1 to about 40 wt. based on the total weight of the liquid.
[0021] In one exemplary embodiment of an immersion technique, the PVB sheet is immersed in an aqueous or solvent-based liquid carrying the modifying agent such that upon retrieval of the sheet and volatilization of the carrier, the sheet surfaces are coated with the agent. In the immersion technique, the concentration of agent in the carrier is preferably about 0.01 to about 20 wt. more preferably about 0.05 to about 5 wt. and even more preferably about 0.1 to about 2 wt. [0022] In one exemplary embodiment of a gravure coating technique, the bifunctional surface modifying agent is disposed dispersed or dissolved) in a liquid carrier, and the liquid carrier is transferred onto the polymer sheet using a gravure coating apparatus. The carrier is subsequently removed from the surface of the polymer sheet, by evaporation.
[0023]1 The resultant PVB sheet having the bifunctional surface modifying agent deposited thereon has a blocking value of at least about 50%, preferably at least about and more preferably at least about 90% less than the blocking value of a polymer sheet comprising PVB resin without the bifunctional surface modifying agent. The clarity of the PVB sheet having a bifunctional surface modifying agent deposited thereon may be determined by measuring the haze value, which is a percentage of transmitted light that is scattered so that its direction deviates more than a specified angle from the direction of the incident beam and may be determined according to ASTM D1003. Preferably, the haze value is less than about more preferably less than about and most preferably less than about 1%.
WO 2004/111116 PCTiUS2004/017953 [0024] The adhesion of the PVB sheet having a bifunctional surface modifying agent deposited on the surface thereof is substantially unaffected by the presence of the bifunctional surface modifying agent. Preferably, the adhesion value (quantification of the tendency of the PVB sheet to adhere to glass) is within about 20%, more preferably within about 10%, and most preferably within about 5% of the adhesion value of a PVB sheet not having a bifunctional surface modifying agent disposed on the surface. Adhesion may be measured by, for example, a pummel adhesion test, which measures the bond strength between the PVB sheet and the glass.
EXAMPLES
[0025] The following tests were used in the Examples: 1. Pummel Adhesion [0026] Two-ply glass laminate samples are prepared with standard autoclave lamination conditions. The laminates are cooled to -17.8 °C and manually pummeled with a hammer to break the glass. All broken glass unadhered to the PVB sheet is then removed, and the amount of glass left adhered to the PVB sheet is visually compared with a set of standards. The standards correspond to a scale in which varying degrees of glass remain adhered to the PVB sheet. In particular, at a pummel standard of zero, no glass is left adhered to the PVB sheet. At a pummel standard of 10, 100% of the glass remains adhered to the PVB sheet..
2. Blocking [0027] This test measures the tendency of the PVB sheet to adhere to itself. In this test, two rectangular filmstrips are cut and placed together in completely overlapping pairs.
The top sheet of each pair is adhered to a piece of tape of a corresponding size. The film pairs are placed centrally between two steel plates and the assembly is subjected to 69 kPa pressure at the temperatures of 7 °C for 24 hours. The strips are then peeled apart in a degree peel test using a peel testing apparatus at a peel speed of 84 inches per minute. The blocking force is quantified in pounds per linear inch (PLI).
WO 2004/111116 PCT/US2004/017953 3. Haze (Clarity) [0028] This test measures the clarity of the laminate made with PVB sheet and is performed in accordance with ASTM D1003-61 (Re-approved 1977)-Procedure A--using Illuminant C, an observer angle of 2 degrees, and an apparatus for measuring the amount of haze is a Hazemeter, Model D25, which is available from Hunterlab.
EXAMPLE 1: Manufacture of PVB Sheet [0029] Plasticized PVB formulation to make PVB sheets comprising 100 parts by weight PVB resin having 16.3 wt.% hydroxyl content calculated as PVOH, 52 parts triethylene glycol di-(2-ethylhexanoate), and other additives including an adhesion control agent, ultraviolet light absorbents, an antioxidant, and other ingredients, was premixed using a high intensity mixer. The plasticized formulation was then melted in an extruder and forced in melt form through a sheeting die having a rectangular die opening at its forward end delimited by a pair of opposing die lips. The temperature of the melt is about 180 The thickness of the extruded sheet is about 30 mils (0.76 mm). Each side of the sheet has a rough surface that allows air to be removed from the interface of the sheet and the glass during lamination process.
EXAMPLE 2: Dip-coating of the PVB Sheet [0030] Dip-coating of the PVB sheet was conducted by dipping the virgin PVB sheet into its respective aqueous solution containing its respective bifunctional surface modifying agent at room temperature for a period of time, 20 seconds, followed by drying. Some of samples were immersed into a fresh water bath after dip-coating. Some of samples were dip-coated at elevated temperatures. The dip-coated samples and the control samples were conditioned to 0.35% moisture level in a conditioning cabinet. Examples of dip-coating conditions, including the type of bifunctional surface modifying agent (surface modifier), concentration of solution, dipping time, and the like are presented in Tables 1-4 respectively, along with the results of the pummel, blocking, and haze tests for the dip-coated samples thereof.
[0031] Table 1 illustrates the results of the pummel, blocking, and haze tests for the samples dip-coated with aqueous solutions of sodium salt of polystyrenesulfonic acid (PSSNa), DSH, or DSNa, followed by a second immersion in water for an equivalent duration to the immersion time noted.
WO 2004/111116 Table 1.
PCT/US2004/017953 Sample Surface Concentration Immersion Blocking Haze Pummel No. Modifier (wt. Time, (sec) Value Adhesion
(PLI)
1. 2.00 0.50 6.6 Control 2. PSSNa 3 2.0 60' 1.86 0.45 6.6 3. DSH 2.0 601 0.06 0.40 4. DSNa 2.0 601 0.75 0.50 3.2 2.96 0.40 6.8 Control 6. DSH 2.0 601 0.42 0.30 4.8 7. DSH 2.0 401 0.27 0.30 8. DSH 2.0 201 0.48 0.30 9. DSH 2.0 201,2 0.48 0.30 DSH 1.0 20' 0.10 0.30 11. DSH 0.5 20' 0.14 0.30 7.3 'Followed by second immersion in water for an equivalent duration to the immersion time noted.
2 Solution temperature increased to 40 OC.
3 PSSNa denotes sodium salt of polystyrenesulfonic acid.
WO 2004/111116 PCT/US2004/017953 [0032] Table 2 illustrates the results of the pummel, blocking, and haze tests for the samples dip-coated with aqueous solutions of DSH having a variety of concentrations for various immersion times at room temperature.
Table 2.
Sample Surface Concentration Immersion Blocking Haze Pummel Modifier (wt. Time, (sec) 12.
Control 13.
14.
16.
17.
18.
DSH
DSH
DSH
DSH
DSH
BSH
Value
(PLI)
4.14 0.10 0.12 0.15 0.24 0.40 0.51 0.40 Adhesion 0.30 0.40 0.40 0.40 0.30 0.40 [0033] Table 3 illustrates the results of the pummel, blocking, and haze tests for the samples dip-coated with 1 wt. aqueous solution of DSH/DSNa mixtures having a variety of DSH/DSNa ratios by weight for various immersion times at room temperature.
WO 2004/111116 PCT/US2004/017953 Table 3.
Sample Surface Concentration Immersion Blocking Haze Pummel No. Modifier (wt. Time, (sec) Value Adhesion
(PLI)
19. 2.80 0.50 6.2 Control 100% DSH 1.0 60 0.03 0.40 9 0% DSNa 21. 100% DSH 1.0 20 0.04 0.40 9 0% DSNa 22. 75% DSH 1.0 60 0.04 0.40 9 DSNa 23. 75% DSH 1.0 20 0.07 0.60 9 DSNa 24. 50% DSH 1.0 60 0.05 0.40 DSNa 50% DSH 1.0 20 0.06 0.50 DSNa [0034] Table 4 illustrates the results of the pummel, blocking, and haze tests for the samples dip-coated with 1 wt. aqueous solutions of DSH/DSNa (or DSMg) mixture having a variety of DSH/DSNa (or DSMg) ratios by weight for 20 seconds at room temperature.
WO 2004/111116 WO 204/11116PCTIUS2004/017953 Table 4.
Sample Surface Concentration Immersion Blocking Haze Pummel No. Modifier (wt. Time, (sec) Value Adhesion
(PUI)
26. 3.50 0.6 6 Control 27. 100% DSH /1 20 0.05 0.5 9 0% DSNa 28. 75% DSH /1 20 0.05 0.5 9 DSNa 29. 50% DSH 1 1 20 0.08 0.5 7.8 DSNa 25% DSII 1 1 20 0.07 0.5 3 DSNa 31. 5% DSH 1 20 0.08 0.5 0 DSNa 32. 0% DSH/ 1 20 0.09 0.5 0 100% DSNa 33. 75% DSHI/ 1 20 0.07 0.5 9 DSMg 34. 50%1 DSH 1 1 20 0.05 0.5 9 DSMg 25% DSHI/ 1 20 0.10 0.5 8 DSMg 36. 5% DSH/ 1 20 0.28 0.5 0 DSMg 37. 0% DSH 1 20 0.23 0.5 0 100% DSMg 38. 2.06 0.4 Control 39 20% DSH/1 1 20 0.02 0.3 WO 2004/111116 PCT/US2004/017953 DSMg 40% DSH/ 1 20 0.04 0.4 8 DSNa 41. 30% DSH 1 20 0.04 0.3 DSNa 42. 20% DSH 1 20 0.07 0.3 DSNa 43. 10% DSH/ 1 20 0.22 0.3 DSNa [0035] The above-described embodiments of PVB sheet having bifunctional surface modifying agents deposited on surfaces thereof are suitable for use in typical PVB interlayer applications for laminated safety glass. Furthermore, the above-described embodiments, because of the modification of the sheet surfaces, are especially useful in manufacturing non-interleaved acoustic PVB interlayer products.
[0036] The PVB sheet as described above also has several advantages over PVB sheet that does not have bifunctional surface modifying agents deposited on surfaces thereof.
First, the PVB sheet having the bifunctional surface modifying agent deposited on surfaces thereof has a considerably reduced tendency to block while maintaining sufficient optical quality and appropriate adhesion properties to glass when the sheet is incorporated into laminated safety glass. By having a reduced tendency to block, the PVB sheet can then be stored and transported with a reduced need for refrigeration or interleaving. Second, because the bifunctional surface modifying agents disclosed above are at least partially compatible with the PVB, additional processing steps such as washing the sheet to remove powder do not need to be performed. Other advantages will be readily apparent to those skilled in the art.
[0037] While the invention has been described with reference to exemplary embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular WO 2004/111116 PCT/US2004/017953 situation or material to the teachings of the invention without departing from the essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiments disclosed as the best mode contemplated for carrying out this invention, but that the invention will include all embodiments falling within the scope of the appended claims.

Claims (12)

1- 1. A polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising, an anti- 00 blocking segment; and a compatibility segment, wherein said bifunctional surface 0- modifying agent comprises the sodium salt of dodecylbenzenesulfonic acid.
2. A laminated safety glass comprising two sheets of glass with an interlayer polymer (N sheet disposed therebetween, wherein the polymer sheet has a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising an anti-blocking segment and a compatibility segment, wherein said bifunctional surface modifying agent comprises the sodium salt of dodecylbenzenesulfonic acid.
3. A polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti- blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a sulfonate radical and wherein said compatibility segment further comprises a positively charged alkali metal counter ion.
4. The polymer sheet of claim 3, wherein said anti-blocking segment comprises a hydrocarbon group comprising a linear hydrocarbon chain, a cyclic group, or a combination of linear hydrocarbon chains and cyclic groups. The polymer sheet of claim 4, wherein said hydrocarbon group comprises about 8 to about 50 carbon atoms.
6. The polymer sheet of claim 4, wherein said cyclic group comprises a benzyl group.
23. Dec. 2008 15:30 Baldwins 64 4 4736712 N f.4079 P. 8 N 0 0 0 7. A laminated safety glass comprising two sheets of glass with an interlayer polymer sheet disposed therebetween, wherein the polymer sheet has a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying C' agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a sulfonate radical and wherein said compatibility 00 segment further comprises an alkali metal positively charged counter ion. 0" 8. The laminated safety glass of claim 7, wherein said anti-blocking segment comprises a hydrocarbon group comprising a linear hydrocarbon chain, a cyclic group, or a combination of linear hydrocarbon chains and cyclic groups. 9. The laminated safety glass of claim 8, wherein said hydrocarbon group comprises about 8 to about 50 carbon atoms. The laminated safety glass of claim 8, wherein said cyclic group comprises a benzyl group. 11. A polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surfac modifying agent comprising: an anti- blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a carboxylate radical and wherein said compatibility segment further comprises a positively charged alkali metal counter ion. 12. The polymer sheet of claim 11, wherein said anti-blocking segment comprises a hydrocarbon group comprising a linear hydrocarbon chain, a cyclic group, or a combination of linear hydrocarbon chains and cyclic groups. 13. The polymer sheet of claim 12, wherein said hydrocarbon group comprises about 8 to about 50 carbon atoms. 14. The polymer sheet of claim 12, wherein said cyclic group comprises a benzyl group. 17 COMS ID No: ARCS-218225 Received by IP Australia: Time 14:30 Date 2008-12-23 o 15. A laminated safety glass comprising two sheets of glass with an interlayer polymer Z sheet disposed therebetween, wherein the polymer sheet has a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said 0compatibility segment comprises a carboxylate radical and wherein said compatibility 00 IDsegment further comprises an alkali metal positively charged counter ion. 16. The laminated safety glass of claim 15, wherein said anti-blocking segment comprises Sa hydrocarbon group comprising a linear hydrocarbon chain, a cyclic group, or a (-i combination of linear hydrocarbon chains and cyclic groups. 17. The laminated safety glass of claim 16, wherein said hydrocarbon group comprises about 8 to about 50 carbon atoms. 18. The laminated safety glass of claim 16, wherein said cyclic group comprises a benzyl group. 19. A polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti- blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a phosphate radical and wherein said compatibility segment further comprises a positively charged alkali metal counter ion. The polymer sheet of claim 19, wherein said anti-blocking segment comprises a hydrocarbon group comprising a linear hydrocarbon chain, a cyclic group, or a combination of linear hydrocarbon chains and cyclic groups. 21. The polymer sheet of claim 20, wherein said hydrocarbon group comprises about 8 to about 50 carbon atoms. O 22. The polymer sheet of claim 20, wherein said cyclic group comprises a benzyl group. 0 Z 23. A laminated safety glass comprising two sheets of glass with an interlayer polymer sheet disposed therebetween, wherein the polymer sheet has a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying 0"agent comprising: an anti-blocking segment; and, a compatibility segment, wherein said 00 IDcompatibility segment comprises a phosphate radical and wherein said compatibility segment further comprises an alkali metal positively charged counter ion. S24. The laminated safety glass of claim 23, wherein said anti-blocking segment comprises a hydrocarbon group comprising a linear hydrocarbon chain, a cyclic group, or a combination of linear hydrocarbon chains and cyclic groups. The laminated safety glass of claim 24, wherein said hydrocarbon group comprises about 8 to about 50 carbon atoms.
26. The laminated safety glass of claim 24, wherein said cyclic group comprises a benzyl group.
27. A polymer sheet, comprising: a bifunctional surface modifying agent disposed onto said polymer sheet, said bifunctional surface modifying agent comprising: an anti- blocking segment; and, a compatibility segment, wherein said compatibility segment comprises a sulfonate, sulfate, carboxylate, or phosphate radical and wherein said compatibility segment further comprises a positively charged alkali metal counter ion; wherein said anti-blocking segment comprises a benzyl group.
28. The polymer sheet of claim 27, wherein said anti-blocking segment comprises about 8 to about 50 carbon atoms.
29. A polymer sheet as claimed in any one of claims 1, 3, 11 to 14, 19 to 22 or 27 to 28 substantially as herein described. O 30. A polymer sheet substantially as herein described with reference to any one of the *Z Examples.
31. A laminated safety glass as claimed in any one of claims 2, 7 to 10, 15 to 18 or 23 to 26 substantially as herein described.
32. A laminated safety glass substantially as herein described with reference to any one of the Examples. 0-
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AU2004247684A1 (en) 2004-12-23
WO2004111116A1 (en) 2004-12-23
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NO20060084L (en) 2006-01-25
EP1639033A1 (en) 2006-03-29
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RU2005141444A (en) 2006-05-27
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TW200505970A (en) 2005-02-16
TWI342320B (en) 2011-05-21

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